A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5486n100



Internal ID22791573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:179218100..179295043hg38UCSC Ensembl
chr4:180139254..180216197hg19UCSC Ensembl
chr4:180376248..180453191hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3876944
hg1976944
hg1876944
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1029967, nsv1022211
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5486n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer